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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099176copy number variation1nstd231human GRCh38.p12 chr1: 10,224,807-12,488,948 , GRCh37 chr1: 10,284,865-12,549,002 TNFRSF8, CLCN6, 64 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7096008copy number variation1nstd102humanUncertain significance GRCh37 chr1: 9,304,994-12,569,078 , GRCh38.p12 chr1: 9,244,935-12,509,024 NMNAT1, DISP3, 91 more genes
    nsv7095738copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,753,911-11,854,615 , GRCh38.p12 chr1: 10,693,854-11,794,558 MAD2L2, HSPE1P24, 33 more genes
    nsv7095737copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,535,024-11,107,264 , GRCh38.p12 chr1: 10,474,967-11,047,207 MASP2, C1orf127, 8 more genes
    nsv7095692copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,698,999-11,907,741 , GRCh38.p12 chr1: 10,638,942-11,847,684 MTHFR, UBIAD1, 36 more genes
    nsv7095543copy number variation1nstd102humanUncertain significance GRCh37 chr1: 9,770,514-11,264,780 , GRCh38.p12 chr1: 9,710,456-11,204,723 DFFA, ANGPTL7, 38 more genes
    nsv7057525inversion1nstd229human GRCh38 chr1: 7,829,944-15,116,659 , GRCh37.p13 chr1: 7,890,004-15,443,155 PEX14, RNU6-304P, 187 more genes
    nsv7052549inversion1nstd229human GRCh38 chr1: 8,322,830-13,737,741 , GRCh37.p13 chr1: 8,382,890-14,064,236 MIR4632, PLOD1, 166 more genes
    nsv7048193inversion1nstd229human GRCh38 chr1: 9,469,567-16,279,388 , GRCh37.p13 chr1: 9,529,626-16,605,883 PRAMEF36P, HNRNPCL3, 193 more genes
    nsv7047983inversion1nstd229human GRCh38 chr1: 5,346,988-12,521,611 , GRCh37.p13 chr1: 5,407,048-12,581,655 THAP3, UBIAD1, 165 more genes
    nsv7046461inversion1nstd229human GRCh38 chr1: 5,352,168-12,521,473 , GRCh37.p13 chr1: 5,412,228-12,581,517 LINC02606, C1orf127, 165 more genes
    nsv6657761copy number variation1nstd229human GRCh38 chr1: 9,535,063-15,753,073 , GRCh37.p13 chr1: 9,595,122-16,079,568 SLC25A34-AS1, TMEM274P, 173 more genes
    nsv6657044copy number variation1nstd229human GRCh38 chr1: 9,097,701-11,036,600 , GRCh37.p13 chr1: 9,157,760-11,096,657 CENPS-CORT, H6PD, 46 more genes
    nsv6639829copy number variation1nstd229human GRCh38 chr1: 11,045,303-11,052,253 , GRCh37.p13 chr1: 11,105,360-11,112,310 MASP2
    nsv6639826copy number variation1nstd229human GRCh38 chr1: 11,037,703-11,046,235 , GRCh37.p13 chr1: 11,097,760-11,106,292 MASP2
    nsv6639694copy number variation1nstd229human GRCh38 chr1: 11,037,701-11,046,300 , GRCh37.p13 chr1: 11,097,758-11,106,357 MASP2
    nsv6639693copy number variation1nstd229human GRCh38 chr1: 11,037,590-11,046,276 , GRCh37.p13 chr1: 11,097,647-11,106,333 MASP2
    nsv6639692copy number variation1nstd229human GRCh38 chr1: 11,036,001-11,046,300 , GRCh37.p13 chr1: 11,096,058-11,106,357 MASP2
    nsv6639690copy number variation1nstd229human GRCh38 chr1: 11,031,026-11,034,479 , GRCh37.p13 chr1: 11,091,083-11,094,536 MASP2, TARDBP
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